Di(1-adamantyl)-n-butylphosphine hydriodide Chemical Properties

storage temp. 

Keep in dark place,Inert atmosphere,Store in freezer, under -20°C

form 

Powder

color 

white

Sensitive 

light sensitive

InChI

InChI=1/C24H39P.HI/c1-2-3-4-25(23-11-17-5-18(12-23)7-19(6-17)13-23)24-14-20-8-21(15-24)10-22(9-20)16-24;/h17-22H,2-16H2,1H3;1H/t17-,18+,19-,20-,21+,22-,23-,24-;

InChIKey

IBXHWLZKSOGUFS-HDWJELNESA-N

SMILES

[H][C@]12C[C@]3(C[C@](C[C@](C3)(C1)[H])(C2)[H])P(CCCC)[C@]12C[C@@]3(C[C@](C1)(C[C@@](C3)(C2)[H])[H])[H].I |&1:1,3,5,7,18,20,22,25,r|

Safety Information

WGK Germany 

3

HS Code 

29319090

Di(1-adamantyl)-n-butylphosphine hydriodide Usage And Synthesis

Chemical Properties

White solid

Uses

Phosphonium salts are ligand precursors for the palladium-catalyzed amination, and Suzuki coupling

Uses

suzuki reaction

General Description

sold in collaboration with Solvias AG

reaction suitability

reaction type: Asymmetric synthesis
reagent type: ligand
reaction type: Arylations
reagent type: ligand
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reagent type: ligand
reaction type: Suzuki-Miyaura Coupling

Di(1-adamantyl)-n-butylphosphine hydriodide(714951-87-8)Related Product Information

• DI-1-ADAMANTYLPHOSPHINE
• Butyldi-1-adamantylphosphine
• Butylmagnesium chloride
• n-Butyllithium
• Butylbenzene
• 1-CHLOROBUTANE-D9
• 3-N-BUTYLPHTHALIDE
• n-Propyl Dioxepin
• N-(n-Butyl)thiophosphoric triamide
• BENZYLDI-1-ADAMANTYLPHOSPHINE
• DI-I-PROPYLPHOSPHINE
• Diphenyl-2-pyridylphosphine
• Di(1-adaMantyl)chlorophosphine
• PHOSPHONIUM IODIDE
• Di(1-adamantyl)-n-butylphosphine hydriodide